Variant #0000673844 (NC_000019.9:g.45922354A>G, NC_000019.9(NM_001983.3):c.525+2T>C (ERCC1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45922354A>G
DNA change (hg38) g.45419096A>G
Published as -
ISCN -
DB-ID ERCC1_000019
Variant remarks -
Reference -
ClinVar ID ClinVar-489383
dbSNP ID -
Origin Germline/De novo (untested)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-07-08 15:03:25 +02:00 (CEST)
Date last edited 2021-03-17 14:24:32 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC1 NM_001983.3 +?/. - c.525+2T>C r.spl? p.?


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